Desonide 51672-1281
Product NDC
51672-1281- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Ointment
- Route
- Topical
- Product Type
- Human Prescription Drug
- Marketing Start
- August 3, 1994
- Listing Expires
- December 31, 2026
- Application
- ANDA074254
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Desonide | .5 mg/g |
Drug Class
Corticosteroid [EPC]Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]
Packaging Options(2)
1 TUBE in 1 CARTON (51672-1281-1) / 15 g in 1 TUBE
1 TUBE in 1 CARTON (51672-1281-3) / 60 g in 1 TUBE